Copy Number Variations (CNVs) Account for 10.8% of Pathogenic Variants in Patients Referred for Hereditary Cancer Testing
在接受遗传性癌症检测的患者中,拷贝数变异(CNV)占致病变异的10.8%。
期刊:Cancer Genomics & Proteomics
影响因子:2.6
doi:10.21873/cgp.20396
Agiannitopoulos, Konstantinos; Pepe, Georgia; Tsaousis, Georgios N; Potska, Kevisa; Bouzarelou, Dimitra; Katseli, Anastasia; Ntogka, Christina; Meintani, Angeliki; Tsoulos, Nikolaos; Giassas, Stylianos; Venizelos, Vassileios; Markopoulos, Christos; Iosifidou, Rodoniki; Karageorgopoulou, Sofia; Christodoulou, Christos; Natsiopoulos, Ioannis; Papazisis, Konstantinos; Vasilaki-Antonatou, Maria; Kabletsas, Eleftherios; Psyrri, Amanta; Ziogas, Dimitrios; Lalla, Efthalia; Koumarianou, Anna; Anastasakou, Kornilia; Papadimitriou, Christos; Ozmen, Vahit; Tansan, Sualp; Kaban, Kerim; Ozatli, Tahsin; Eniu, Dan Tudor; Chiorean, Angelica; Blidaru, Alexandru; Rinsma, Marrit; Papadopoulou, Eirini; Nasioulas, George